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Biology Department Western Wyoming Community College PHYSIOLOGY OF CARDIAC HYPERTROPHY IN SEVERELY IRON DEFICIENT RATS USING PRESSURE- VOLUME LOOPS BY: JACQUIE ZADRA, EMILY THOMPSON, AND ASHLEY WEIGEL FACULTY MENTOR: BUD CHEW, PH.D.
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Enlargement of the heart Can either be adaptive or pathological Adaptive hypertrophy is seen in aerobic athletes Pathological hypertrophy is seen in diseases of the heart such as congestive heart failure CARDIAC HYPERTROPHY
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Adaptive hypertrophy Increased cardiac output Increased heart chamber size Healthy heart wall muscle Pathological Hypertrophy Decreased cardiac output No increase in heart chamber size Fibrotic heart wall Due to increase in collagen ADAPTIVE VS PATHOLOGICAL HYPERTROPHY
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PROLONGED IRON DEFICIENCY CAUSES CARDIAC HYPERTROPHY
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12 weeks of iron deficiency Morphological indications of failure Apoptosis stimulated Cardiac function of this hypertrophy is poorly understood CURRENT UNDERSTANDING OF CARDIAC HYPERTROPHY FROM IRON DEFICIENCY Ref: Dong et al., 2007.
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We hypothesized that four weeks of iron deficiency would result in failing cardiac function and decreased sympathetic neurotransmitter stores. HYPOTHESIS
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Two groups Sprague-Dawley Rats Four rats fed iron deficient diet (AIN-93G without iron) Four rats fed control diet (AIN- 93G) Four weeks of the respective dietary intervention Cardiac pressure-volume loop protocol Plasma and hearts frozen for HPLC analysis EXPERIMENTAL DESIGN
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2 femoral vein catheters for drug infusion 1 jugular vein catheter for saline calibration 1 carotid artery exposure for PV loop transducer Inserted into the carotid artery and passed into the left ventricle PV LOOP PROTOCOL: SURGERY
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Aortic pressure measurements and baseline cardiac function data Inferior Vena Cava occlusion for measure of contractility Saline calibration for parallel conductance subtraction Dopamine infusion Atenolol infusion Second baseline data Heparinized rat to prevent blood clotting Cuvette calibration for measure of true blood volume Collect microhematocrit samples Centrifuge remaining blood for plasma Freeze plasma and hearts for HPLC analysis PV-LOOP PROTOCOL: DATA COLLECTION
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RESULTS: IRON DEFICIENCY Group Hematocrit (Percent) *p<0.05 Hematocrit Group Mass (grams) *p<0.05 Body Mass
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RESULTS: CARDIAC HYPERTROPHY gmgm -1 Group HeartBody Mass -1 Ratio *p<0.05 Iron Deficient Control
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PRESSURE-VOLUME LOOPS Stroke Volume Ejection Isovolumic Relaxation End Diastolic Volume Filling Isovolumic Contraction End Systolic PV relationship (ESPVR) Cardiac output= (SV)(HR) Heart Rate
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RESULTS: PRESSURE-VOLUME LOOPS Iron Deficient-FailingIron Deficient-AdaptiveControl
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CO=HR*SV RESULTS: PRESSURE-VOLUME LOOPS uLmin -1 Group *p<0.05 Cardiac Output
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RESULTS: PRESSURE VOLUME LOOPS Group Heart Rate bpm Group *p<0.05 Stroke Volume uL
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Stroke volume is affected by three factors: (1) Preload End diastolic volume RESULTS: PRESSURE VOLUME LOOPS Group *p<0.05 End Diastolic Volume uL
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RESULTS: PRESSURE-VOLUME LOOPS (2) Contractility Sympathetic nervous system Ejection fraction Frank-Starling Law of The Heart Group Percent *p<0.05 Ejection Fraction
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Control rat ejection fraction averaged 55% Iron deficient rat ejection fraction averaged 93% ESPVR AS A MEASURE OF CONTRACTILITY
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RESULTS: PRESSURE-VOLUME LOOPS Group mmHgs -1 dpdt -1 Max
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(3) Afterload Aortic diastolic pressure RESULTS: PRESSURE-VOLUME LOOPS Group Pressure (mmHg) Aortic Diastolic Pressure
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PROLONGED IRON DEFICIENCY CAUSES CARDIAC HYPERTROPHY
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HIGH PERFORMANCE LIQUID CHROMATOGRAPHY HPLC is a technique used to separate and quantify chemical compounds in a liquid medium Used to determine concentration of norepinephrine in extracted plasma
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RESULTS: HPLC Group NE (ugml -1 ) Plasma Norepinephrine Concentration
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CONCLUSION: 3 ADAPTIVE ID HEARTS, 1 FAILING ID HEART
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Thanks to Wyoming INBRE for funding our research ACKNOWLEDGMENTS
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